HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323523Generated: October 31, 2026
Chloroacetic Acid → [(5-Methyl-1,3,4-thiadiazol-2-yl)sulfanyl]acetic acid
https://huagongshe.com/reaction/323523
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetic Acid | HCID 300 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178434161 | HCID 178434161 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | [(5-Methyl-1,3,4-thiadiazol-2-yl)sulfanyl]acetic acid | HCID 589580 | 75% |
Reaction Steps
Aqueous solution of sodium hydroxide 8.8 g (0.22 mol) in 15 ml of water was added to a mixture of 2-mercapto-5-methyl-1,3,4-thiadiazole 26.4 g (0.20 mol), chloroacetic acid 27.0 g (0.22 mol) and ethanol 300 ml with stirring at room temperature. After 20 minutes of stirring it was heated to 50° C., and further aqueous solution of sodium hydroxide 8.8 g (0.22 mol) in 15 ml of water was added slowly drop by drop. After stirring for 3 hours at 50° C., it was cooled to room temperature, and water was added till reaction liquid became uniform. Hydrochloric acid was added for neutralization. Prepared crystal was collected by filtration and 28.7 g (0.150 mol) of 2-carboxymethylthio-5-methyl-1,3,4-thiadiazole was obtained by recrystallization in methanol. Yield 75%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06214533B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-3904dc23cf5543ca916a97de073c3d95 |
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| Source note | uspto-grants-2001_04 |
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